Loss of Geminin induces rereplication in the presence of functional p53

被引:214
作者
Melixetian, M
Ballabeni, A
Masiero, L
Gasparini, P
Zamponi, R
Bartek, J
Lukas, J
Helin, K
机构
[1] European Inst Oncol, Dept Expt Oncol, I-20141 Milan, Italy
[2] FIRC, Inst Mol Oncol, I-20122 Milan, Italy
[3] Danish Canc Soc, Inst Canc Biol, DK-2100 Copenhagen, Denmark
[4] Biotech Res & Innovat Ctr, DK-2100 Copenhagen, Denmark
关键词
DNA replication; genomic instability; Geminin; p53; S phase checkpoint;
D O I
10.1083/jcb.200403106
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Strict regulation of DNA replication is essential to ensure proper duplication and segregation of chromosomes during the cell cycle, as its deregulation can lead to genomic instability and cancer. Thus, eukaryotic organisms have evolved multiple mechanisms to restrict DNA replication to once per cell cycle. Here, we show that inactivation of Geminin, an inhibitor of origin licensing, leads to rereplication in human normal and tumor cells within the same cell cycle. We found a CHK1-dependent checkpoint to be activated in rereplicating cells accompanied by formation of gammaH2AX and RAD51 nuclear foci. Abrogation of the checkpoint leads to abortive mitosis and death of rereplicated cells. In addition, we demonstrate that the induction of rereplication is dependent on the replication initiation factors CDT1 and CDC6, and independent of the functional status of p53. These data show that Geminin is required for maintaining genomic stability in human cells.
引用
收藏
页码:473 / 482
页数:10
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